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. 2022 Jun 9;13:884530. doi: 10.3389/fimmu.2022.884530

Figure 2.

Figure 2

Keratinocyte-derived sEVs are enriched in glycoproteins involved in adhesion in steady state and in AD milieu. (A) Enrichment of adhesion proteins involved in cell adhesion in sEVNHEK secreted in steady-state keratinocytes; Reactome - Gene Ontology terms re-analysis of the data available from Chavez-Muñoz et al. (28); (B) enrichment of adhesion proteins involved in cell adhesion in sEVNHEK secreted by NHEKs exposed to AD milieu as identified by Reactome - Gene Ontology terms analysis; (C) interaction network for sEV adhesion-relevant proteins identified in sEV0.06NHEK and sEV1.5NHEK; (D) cell adhesion-relevant glycoproteins identified by mass spec in sEV0.06NHEK and sEV1.5NHEK; (E) Reactome-Gene Ontology identified term enrichment for the proteins in sEV0.06NHEK and sEV1.5NHEK; FDR, False Discovery Rate; N.B. classical exosomal glycoprotein markers are included in the supplementary data ( Figure S2D ); mass spectrometry data based on n=3 biological replicates.